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About:hqqu

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Huiqi Qu has a background as a physician trained in internal medicine and a PhD in Experimental Medicine (Endocrinology). His research applies human genetics and multi-omics to complex and pediatric diseases, including GWAS, polygenic risk scores (PRS), single-cell transcriptomics, and integrative genomics to support precision medicine and clinical translation.

Posts by hqqu :

  • Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS) (Contributed by Dr. Nan Wu), Posted on May 8, 2020 by hqqu in Uncategorized
  • 15q11.2 deletion is enriched in patients with total anomalous pulmonary venous connection (Contributed by Dr. Bo Wang), Posted on May 7, 2020 by hqqu in Uncategorized
  • Comprehensive genetic sequence and copy number analysis for Charcot-Marie-Tooth disease in a Canadian cohort of 2517 patients (Contributed by Dr. Bekim Sadikovic), Posted on May 7, 2020 by hqqu in Uncategorized
  • Understanding polygenic models, their development and the potential application of polygenic scores in healthcare (Contributed by Dr. Chantal Babb de Villiers), Posted on May 7, 2020 by hqqu in Uncategorized
  • Uptake of pre-symptomatic testing for BRCA1 and BRCA2 is age, gender, offspring and time dependent (Contributed by Dr. Claire Forde), Posted on May 1, 2020 by hqqu in Uncategorized
  • Novel genetic characterisation and phenotype correlation in von Hippel-Lindau (VHL) disease based on the Elongin C binding site: a large retrospective study (Contributed by Dr. Haibiao Xie), Posted on April 18, 2020 by hqqu in Uncategorized
  • Identifying novel oncogenic RET mutations and characterising their sensitivity to RET-specific inhibitors (Contributed by Dr. Yu Yao), Posted on April 14, 2020 by hqqu in Uncategorized
  • Identification of known and unknown genes associated with mitral valve prolapse using an exome slice methodology (Contributed by Dr. Aniek van Wijngaarden), Posted on April 14, 2020 by hqqu in Uncategorized
  • Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank (Contributed by Dr. William Davies), Posted on March 17, 2020 by hqqu in Uncategorized
  • A homozygous UBA5 pathogenic variant causes a fatal congenital neuropathy (Contributed by Dr. Macarena Cabrera), Posted on March 17, 2020 by hqqu in Uncategorized
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